Promotion of allograft survival by CD4+ CD25+ regulatory T cells:: Evidence for in vivo inhibition of effector cell proliferation

被引:98
作者
Lee, K
Moore, DJ
Jarrett, BP
Lian, MM
Deng, SP
Huang, XL
Markmann, JW
Chiaccio, M
Barker, CF
Caton, AJ
Markmann, JF
机构
[1] Hosp Univ Penn, Dept Surg, Harrison Dept Surg Res, Philadelphia, PA 19104 USA
[2] Wistar Inst Anat & Biol, Philadelphia, PA 19104 USA
关键词
D O I
10.4049/jimmunol.172.11.6539
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells preserve tolerance to peripheral self-Ags and may control the response to allogeneic tissues to promote transplantation tolerance. Although prior studies have demonstrated prolonged allograft survival in the presence of regulatory T cells (T-reg), data documenting the capacity of these cells to promote tolerance in inummocompetent transplant models are lacking, and the mechanism of suppression in vivo remains unclear. We used a TCR transgenic model of allograft rejection to characterize the in vivo activity of CD4(+)CD25(+) T-reg. We demonstrate that graft Ag-specific T-reg effectively intercede in the rejection response of naive T cells to established skin allografts. Furthermore, CFSE labeling demonstrates impaired proliferation of naive graft Ag-specific T cells in the draining lymph node in the presence of T-reg. These results confirm the efficacy of T-reg in promoting graft survival and suggest that their suppressive action is accomplished in part through inhibition of proliferation.
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页码:6539 / 6544
页数:6
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